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Volumn 15, Issue 3, 2003, Pages 242-250

Conformational preferences in diastereomeric (5s)-methyl-3-(o-aryl)-2,4-oxazolidinediones

Author keywords

Barrier to rotation; Facial selectivity; Hindered rotation; Separation of diastereomers; Thermal interconversion; Thermodynamic enrichment

Indexed keywords

BROMINE; CHLOROFORM; DEUTERIUM; IODINE DERIVATIVE; METHANOL; METHYL GROUP; NAPHTHYL GROUP; OXAZOLIDINEDIONE DERIVATIVE;

EID: 0037282352     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10189     Document Type: Article
Times cited : (18)

References (9)
  • 1
    • 37049076153 scopus 로고
    • The enantiomers of N-aryl-2-thioxo-4-oxazolidinones and N-arylrhodanines. Investigation by liquid chromatography, circular dichroism and thermal racemization
    • Doǧan I, Pustet N, Mannschreck A. The enantiomers of N-aryl-2-thioxo-4-oxazolidinones and N-arylrhodanines. Investigation by liquid chromatography, circular dichroism and thermal racemization. J Chem Soc Perkin Trans 2 1993;1557-1560.
    • (1993) J Chem Soc Perkin Trans 2 , pp. 1557-1560
    • Doǧan, I.1    Pustet, N.2    Mannschreck, A.3
  • 2
    • 0026757351 scopus 로고
    • Synthesis and NMR studies of chiral 4-oxizolidinones and rhodanines
    • Doǧan I, Burgemeister T, Içli S, Mannschreck A. Synthesis and NMR studies of chiral 4-oxizolidinones and rhodanines. Tetrahedron 1992; 48:7157-7164.
    • (1992) Tetrahedron , vol.48 , pp. 7157-7164
    • Doǧan, I.1    Burgemeister, T.2    Içli, S.3    Mannschreck, A.4
  • 4
    • 84986760752 scopus 로고
    • 13C NMR studies on 3-aryl-5-alkyl-2,4-oxazolidinediones. The magnetic non-equivalence of isomeric nuclei
    • 13C NMR studies on 3-aryl-5-alkyl-2,4-oxazolidinediones. The magnetic non-equivalence of isomeric nuclei. Org Mag Reson 1979;12:178-182.
    • (1979) Org Mag Reson , vol.12 , pp. 178-182
    • Içli, S.1
  • 5
    • 0000061302 scopus 로고
    • New York: John Wiley & Sons
    • Smith PAS. Organic reactions. New York: John Wiley & Sons; 1946;3: 337-450.
    • (1946) Organic Reactions , vol.3 , pp. 337-450
    • Smith, P.A.S.1
  • 9
    • 0013357772 scopus 로고    scopus 로고
    • NMR analysis of restricted internal rotation in 2-substituted-2,3-dihydro-3-o-tolyl(chlorophenyl)-4(1H) quinazolinones
    • Noto R, Gruttadauria M, Pace A. NMR analysis of restricted internal rotation in 2-substituted-2,3-dihydro-3-o-tolyl(chlorophenyl)-4(1H) quinazolinones. J Heterocyclic Chem 1996;33:1067-1071.
    • (1996) J Heterocyclic Chem , vol.33 , pp. 1067-1071
    • Noto, R.1    Gruttadauria, M.2    Pace, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.